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Summary Literature (0)
DOID:0110238 - cataract 18

Disease Ontology Definition:A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3.

Synonyms: CATC2, CTRCT18, autosomal recessive congenital cataract 2, cataract 18 autosomal recessive,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012395 - cataract 18


Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive disease (is_a), cataract (is_a)